List of variants in gene WT1 reported as likely pathogenic by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.965+1G>A	rs771527206	0.00001
NM_024426.6(WT1):c.1016+1G>A	rs2133032244
NM_024426.6(WT1):c.1016+2T>G	rs1852674417
NM_024426.6(WT1):c.1114-1G>T	rs1851976798
NM_024426.6(WT1):c.1297T>G (p.Cys433Gly)	rs121907905
NM_024426.6(WT1):c.1406A>G (p.Asp469Gly)	rs121907902
NM_024426.6(WT1):c.1447+2T>C	rs1851829439
NM_024426.6(WT1):c.965+2T>C

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